Structure analysis

Crystal Structure of Hydroxycinnamoyl-CoA Hydratase-Lyase

X-ray diffraction
1.8Å resolution
Source organism: Pseudomonas fluorescens
Assembly composition:
hetero hexamer (preferred)
Entry contents: 3 distinct polypeptide molecules

Assemblies

Assembly 1
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Multimeric state: hetero hexamer
Accessible surface area: 46174.11 Å2
Buried surface area: 28990.46 Å2
Dissociation area: 4,823.7 Å2
Dissociation energy (ΔGdiss): 37.4 kcal/mol
Dissociation entropy (TΔSdiss): 15.96 kcal/mol
Symmetry number: 6
PDBe Complex ID: PDB-CPX-130664
Assembly 2 (preferred)
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Multimeric state: hetero hexamer
Accessible surface area: 45627.48 Å2
Buried surface area: 29031.62 Å2
Dissociation area: 4,822.92 Å2
Dissociation energy (ΔGdiss): 34.97 kcal/mol
Dissociation entropy (TΔSdiss): 15.96 kcal/mol
Symmetry number: 6
PDBe Complex ID: PDB-CPX-130664

Macromolecules

Chain: A
Length: 276 amino acids
Theoretical weight: 31.01 KDa
Source organism: Pseudomonas fluorescens
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: O69762 (Residues: 1-276; Coverage: 100%)
Pfam: Enoyl-CoA hydratase/isomerase
InterPro:
CATH:

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Chains: B, C, D, E, F, G, H, J, K, L
Length: 276 amino acids
Theoretical weight: 31.04 KDa
Source organism: Pseudomonas fluorescens
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: O69762 (Residues: 1-276; Coverage: 100%)
Pfam: Enoyl-CoA hydratase/isomerase
InterPro:
CATH:

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Chain: I
Length: 276 amino acids
Theoretical weight: 31.04 KDa
Source organism: Pseudomonas fluorescens
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: O69762 (Residues: 1-276; Coverage: 100%)
Pfam: Enoyl-CoA hydratase/isomerase
InterPro:
CATH:

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